| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086710-112086921 | Rare:90; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112225999-112226274 | Common:1; Rare:44 | ||||
| chr11:112226307-112226475 | Rare:74 | ||||
| chr11:113314454-113314602 | Rare:51 | ||||
| chr11:113875493-113875775 | Common:4; Rare:103 | ||||
| chr11:114059410-114059930 | Common:1; Rare:105 | ||||
| chr11:114296256-114296669 | Rare:88 | ||||
| chr11:114399755-114400035 | Common:1; Rare:68 | ||||
| chr11:114400427-114400766 | Common:2; Rare:130 | ||||
| chr11:116772949-116773088 | Rare:53 | ||||
| chr11:116787979-116788061 | Rare:28 | ||||
| chr11:116791810-116792015 | Common:1; Rare:53 | ||||
| chr11:116792410-116792743 | Common:2; Rare:56 | ||||
| chr11:116829674-116830070 | Common:3; Rare:81 | ||||
| chr11:116830417-116830891 | Common:4; Rare:164; Clinvar (benign):1; Clinvar (pathogenic):3 |